What is the treatment for pustular lesions in children?

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Treatment of Pustular Lesions in Children

Immediate Diagnostic Approach

The first priority is to distinguish infectious from non-infectious pustular eruptions, as infectious causes require immediate antimicrobial therapy while non-infectious causes may worsen with inappropriate treatment. 1

Essential Rapid Diagnostic Tests

  • Perform a Tzanck smear first - this is the single most important rapid diagnostic test that detects herpetic infections (multinucleated giant cells) and differentiates infectious from non-infectious pustular eruptions (eosinophils vs neutrophils). 1
  • Gram stain should be performed immediately to detect bacterial infections, particularly Staphylococcus aureus and Listeria monocytogenes in neonates. 1
  • Potassium hydroxide (KOH) preparation is essential to identify fungal infections, particularly candidiasis. 1
  • Bacterial, viral, and fungal cultures should be obtained before initiating therapy. 1

Treatment Algorithm by Etiology

Infectious Pustular Lesions

For bacterial impetigo or localized staphylococcal infections, apply mupirocin ointment 2% three times daily to affected areas. 2

  • The treated area may be covered with gauze dressing if desired. 2
  • Re-evaluate patients who do not show clinical response within 3-5 days. 2
  • Avoid use on mucosal surfaces and discontinue if sensitivity or chemical irritation occurs. 2
  • For systemic bacterial infections or sepsis, initiate appropriate intravenous antibiotics immediately based on culture results. 1

Non-Infectious Pustular Psoriasis

Mild to Moderate Pustular Psoriasis

Begin with topical calcineurin inhibitors (tacrolimus 0.1%) for facial and genital involvement, as these show excellent improvement within 30 days without the risk of skin atrophy. 3

  • Combination therapy with topical vitamin D analogs and topical corticosteroids is effective for plaque-type pustular psoriasis. 3
  • Use moderately potent (class III) topical corticosteroids for body lesions to balance efficacy with safety. 4
  • Avoid high-potency or ultra-high-potency corticosteroids in children 0-6 years due to high risk of HPA axis suppression from their elevated body surface area-to-volume ratio. 3

Severe, Unstable, or Generalized Pustular Psoriasis

Acitretin is recommended as the first-line systemic therapy for pustular psoriasis in children at 0.1-1 mg/kg/day, with response typically seen within 3 weeks. 5

  • Acitretin is particularly effective for pustular variants and is non-immunosuppressive. 5
  • Acitretin combined with narrowband UVB phototherapy is synergistic and allows dose reduction of both agents. 5
  • Monitor for mucocutaneous dryness (most common side effect) and hyperlipidemia (transient and dose-dependent). 5
  • Absolutely avoid acitretin in female adolescents approaching childbearing potential, as it remains stored in the body for up to 3 years when reverse-esterified to etretinate in the presence of alcohol. 5, 4

For rapid control of severe, unstable pustular psoriasis, cyclosporine 2-5 mg/kg/day achieves skin clearance in approximately 4 weeks. 5

  • Cyclosporine is excellent for crisis management and rapidly progressive disease. 5
  • Initiate at the higher end of the dosing range and reduce to the lowest effective maintenance dose. 5
  • Use as short-term intermittent therapy rather than long-term maintenance. 6

Refractory Pustular Psoriasis

Infliximab 5 mg/kg IV at weeks 0,2, and 6, then every 8 weeks is recommended for severe pustular psoriasis unresponsive to other systemic medications, rapidly progressive, unstable, or life-threatening disease. 5

  • Infliximab can be used as monotherapy or combined with methotrexate. 5
  • This is particularly effective for pustular variants that have failed conventional systemic therapy. 5

Benign Transient Neonatal Pustulosis

For erythema toxicum neonatorum, transient neonatal pustular melanosis, and infantile acropustulosis, no treatment is required as these are self-limited conditions. 1, 7

  • These diagnoses spare the neonate from invasive sepsis evaluation, harmful antibiotic therapy, and prolonged hospitalization. 1
  • Reassurance and observation are appropriate once infectious causes are excluded. 1

Critical Safety Considerations

Monitoring Requirements

  • Routine clinical and laboratory monitoring is mandatory during systemic therapy with acitretin, cyclosporine, or biologics. 5
  • For biologics, monitor for injection site reactions and increased infection risk. 5
  • Screen for latent tuberculosis before initiating biologic therapy, particularly TNF-α inhibitors. 5

Common Pitfalls to Avoid

  • Never abruptly discontinue high-potency corticosteroids, as this causes significant rebound flares. 3
  • Do not use mupirocin on mucosal surfaces or in patients with moderate-to-severe renal impairment due to polyethylene glycol absorption. 2
  • Do not delay infectious disease workup in any neonate with pustules - sepsis must be ruled out first. 1
  • Avoid methotrexate in female adolescents without reliable contraception due to teratogenicity (pregnancy category X). 5

Age-Specific Precautions

  • Infants and children 0-6 years require extreme caution with topical corticosteroids and limited quantities with clear application instructions. 3
  • Adolescents approaching childbearing potential should avoid acitretin and use methotrexate only with reliable contraception. 5, 4
  • Phototherapy requires patient cooperation and is generally reserved for children old enough to tolerate 2-3 weekly sessions. 4

References

Guideline

Pediatric Dermatitis and Psoriasis Treatment

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Treatment of Eczema and Psoriasis in Adolescents

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Childhood psoriasis.

Indian journal of dermatology, venereology and leprology, 2010

Research

Pustular skin disorders: diagnosis and treatment.

American journal of clinical dermatology, 2002

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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